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The ability of a limited metabolic assessment to identify pediatric stone formers with metabolic abnormalities
K H Chan1, E A Moser2, B M Whittam3
1Department of Urology, 535 Barnhill Dr. Indianapolis, IN, 46202, USA; Center for Pediatric and Adolescent Comparative Effectiveness Research and Department of Biostatistics, 410 W. 10th St. Suite 2000, Indianapolis, IN 46202, USA.
Insights
A limited urinary metabolic evaluation effectively identifies most metabolic abnormalities in pediatric kidney stone patients. This approach can simplify diagnosis and reduce healthcare costs for first-time stone formers.
Area of Science:
- Pediatric Nephrology
- Urology
- Metabolic Disorders
Background:
- Pediatric kidney stone evaluation guidelines recommend comprehensive metabolic assessment after the first stone event.
- Previous research highlighted hypercalciuria and low urine volume as common abnormalities.
- Recent findings indicate hypocitraturia is the most prevalent metabolic abnormality in pediatric stone formers.
Purpose of the Study:
- To test the hypothesis that a limited urinary metabolic evaluation can detect the majority of clinically significant metabolic abnormalities in pediatric stone formers.
- To compare the diagnostic yield of a limited four-parameter evaluation against a complete metabolic profile.
- To determine the number and types of abnormalities missed by a limited evaluation.
Main Methods:
- Retrospective analysis of 80 pediatric patients (<18 years) with renal/ureteral calculi and at least one 24-hour urinary metabolic profile.
- Exclusion criteria included bladder stones and inadequate urine collection (under/overcollection, missing creatinine).
- Comparison of a limited evaluation (24-h calcium, citrate, oxalate, urine volume) with a complete metabolic profile.
Main Results:
- Hypocitraturia (69.6%), low urine volume (52.5%), and hypercalciuria (22.5%) were the most common abnormalities.
- The limited evaluation demonstrated 87.5% sensitivity.
- Ten patients had abnormalities missed by the limited evaluation, including high pH, abnormal phosphorus, and low magnesium/potassium.
Conclusions:
- A simplified, limited urinary metabolic evaluation can identify most clinically significant metabolic abnormalities in pediatric stone formers.
- This streamlined approach has the potential to simplify metabolic evaluations and reduce healthcare expenditures.
- A significant proportion of patients (approximately two-thirds) provided inadequate urine specimens, underscoring the importance of proper collection techniques.
Introduction:
American Urological Association guidelines recommend a urinary metabolic evaluation after the first stone event in all pediatric stone patients. Prior studies identified hypercalciuria and urine hypovolemia as the most common abnormalities in children with urolithiasis. Recent data suggest that hypocitraturia is most prevalent. It was hypothesized that a limited evaluation would detect the majority of clinically significant metabolic abnormalities in pediatric stone formers.
Material And Methods:
A retrospective analysis of all children (<18 years of age) with renal/ureteral calculi evaluated at the study institution from 2005 to 2015 was performed. Children with ≥ one 24-h urinary metabolic profile after a clinical visit for renal/ureteral calculi were included. Those with bladder stones and those with undercollection or overcollection or missing urinary creatinine were excluded. Demographics and data from the first urinary metabolic profile and stone analyses were collected. The sensitivity, specificity, and positive and negative predictive value (NPV) of a limited urinary metabolic evaluation consisting of four parameters (24-h calcium, citrate, and oxalate and low urinary volume) were compared to a complete urinary metabolic profile. The number and type of metabolic abnormalities that would have been missed with this limited evaluation weredetermined.
Results:
Of 410 patients, 21 were excluded for age ≥18 years, 13 for bladder stones, 248 for overcollections, 38 for undercollections, and 10 for missing creatinine. This left 80 patients for inclusion: median age 11.4 years, 60% female, and 96.3% white. Of the entire cohort, 69.6% had hypocitraturia, 52.5% had low urine volume, and 22.5% had hypercalciuria. Sensitivity was 87.5%. Specificity could not be calculated because no patients had a normal complete metabolic evaluation. The NPV was zero, and the positive predictive value was 100%, but these are artifacts resulting from the absence of patients with a normal complete metabolic evaluation. Of the 80 patients, 10 had at least one abnormality missed by a limited metabolic evaluation (Table 1). The missed abnormalities were high pH (n = 6), abnormal 24-h phosphorus (low in 1 patient and high in 1 patient), low 24-h magnesium (n = 3), low 24-h potassium (n = 3), and high 24-h sodium (n = 4).
Discussion:
A limited urinary metabolic evaluation would have detected the vast majority of clinically significant metabolic abnormalities in the study sample. Approximately two-thirds of the study patients submitted inadequate 24-h urine specimens.
Conclusions:
A simplified approach to metabolic evaluation in first-time stone formers with a stone analysis available was proposed. This streamlined approach could simplify the metabolic evaluation and reduce health care costs.
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